Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7246865
MYO9B
19 17108295 intron variant G/A snv 0.36 1
rs17213965
MYH11
16 15788110 intron variant C/T snv 0.24 1
rs1051921
MLXIPL
0.925 0.120 7 73593613 3 prime UTR variant G/A snv 0.15 6
rs55747707
MLXIPL
7 73623036 intron variant G/A snv 0.16 1
rs12731740
MIR29B2CHG
1 207851475 intron variant C/T snv 9.1E-02 1
rs11897119
MEIS1
2 66544868 intron variant T/A;C snv 1
rs2229616
MC4R
0.732 0.200 18 60372043 missense variant C/T snv 1.6E-02 1.6E-02 2
rs8070723
MAPT
0.851 0.240 17 46003698 intron variant A/G snv 0.18 5
rs2820464
LYPLAL1-AS1
1 219519878 intergenic variant G/A;C snv 1
rs15285
LPL
1.000 0.040 8 19967156 3 prime UTR variant C/T snv 0.36 1
rs12440667
LOXL1
1.000 0.040 15 73939098 intron variant C/A;T snv 1
rs9369425
LOC107986598
0.882 0.160 6 43843237 downstream gene variant G/A snv 0.66 3
rs1993709
LOC105378797
1.000 0.080 1 72372846 intron variant A/G snv 0.85 1
rs987763
LOC105377989
6 126960402 intron variant C/A;T snv 1
rs12110693
LOC105377979
6 121837124 intergenic variant G/A snv 0.23 1
rs718314
LOC105369705
0.882 0.120 12 26300350 intron variant A/G snv 0.27 2
rs1294410
LOC101928004
6 6738519 intron variant T/C snv 0.65 1
rs1294421
LOC101928004
1.000 0.040 6 6742916 upstream gene variant T/A;C;G snv 1
rs1055144
LOC100506236
1.000 0.040 7 25831489 non coding transcript exon variant C/T snv 0.16 2
rs1876829
LINC02210-CRHR1 ; MAPT-AS1 ; CRHR1
1.000 0.040 17 45834077 intron variant T/C snv 0.15 0.14 2
rs900400
LINC02029
0.925 0.080 3 157080986 upstream gene variant T/C snv 0.36 1
rs4640244
KCNJ12
17 21380911 intron variant A/G snv 0.33 1
rs7637773
IGF2BP2
1.000 0.080 3 185797847 intron variant G/A snv 0.38 1
rs2277339
HSD17B6 ; PRIM1
12 56752285 missense variant T/G snv 0.12 0.14 1
rs2894204
HLA-C
1.000 0.040 6 31269284 intron variant C/A;T snv 1